Aqueous coating compositions containing acetoacetyl-functional polymers, coatings, and methods

ABSTRACT

Aqueous coating compositions that include polymers having one or more of the following acetoacetyl-functional groups: 
                         
wherein R 1  is a C1 to C22 alkylene group and R 2  is a C1 to C22 alkyl group.

This application claims the benefit of the U.S. Provisional ApplicationNo. 60/636,921, filed Dec. 17, 2004, which is incorporated by referencein its entirety.

BACKGROUND

There is a significant need for lower VOC-containing (volatile organiccompound-containing) and formaldehyde-free systems in the coatingsindustry due to increasing environmental restrictions. Aqueous-basedthermoplastic coatings, such as latexes can be applied with low levelsof solvents and formaldehyde, but they do not have the hardness andchemical resistance required for many applications. Chemicallycrosslinked coatings, such as aqueous-based melamine cured coatings,that give good block and chemical resistance contain low levels offormaldehyde. For interior applications such as coatings for kitchencabinets, however, many consumers desire “Green” systems, which arecarcinogen free. Other crosslinking technologies such as blockedisocyanates or ethylenically unsaturated compounds also achieve thedesired performance; however, these technologies are often costprohibitive or highly irritating either to skin, eyes, or both.

Thus, what is needed are coating compositions that have one or more ofthe following properties: high performance, low VOC levels,substantially no formaldehyde content, and low irritation levels.

SUMMARY

The present invention provides aqueous coating compositions that includepolymers having one or more of the following acetoacetyl-functionalgroups:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup. Preferably, R¹ is a C1 to C4 alkylene group and R² is a C1 to C4alkyl group, and more preferably, R¹ is methylene (—CH₁₂—) and R² ismethyl (—CH₃).

Such functionalized polymers are desirable because they can become partof a crosslinked network, thereby providing advantageous coatingproperties. Preferred compositions also possess one or more of thefollowing properties: low VOC levels, substantially no formaldehydecontent, high performance, and low irritation levels.

Such coating compositions can be coated onto a substrate and dried(e.g., cured), as with a paint, for example. Desirable performancecharacteristics of the coating include chemical resistance, abrasionresistance, hardness, gloss, reflectivity, appearance, or combinationsof these characteristics, and other similar characteristics. Polymershaving one or more acetoacetyl-functional groups as described above canbe latex polymers or water-dispersible polymers.

Preferred coating compositions include no more than 10 weight percent(wt-%) (more preferably, no more than 7 wt-%) volatile organic compounds(VOC), based on the total weight of the composition.

Preferred acetoacetyl-functional polymers include anacetoacetyl-functional polyurethane, epoxy, polyamide, chlorinatedpolyolefin, acrylic, oil-modified polymer, polyester, or mixtures orcopolymers thereof. Preferably, acetoacetyl-functional polymers areprepared at a pH no more than 8.5, more preferably no more than a pH of8.0, and most preferably at a pH no more than 7.8. In certainembodiments, the acetoacetyl-functional polymer is anacetoacetyl-functional latex polymer. Preferably, theacetoacetyl-functional latex polymer includes latex particles having anaverage particle size (i.e., the average of the longest dimension of theparticles, typically, a diameter) of less than 75 nm as measured by aCoulter N4 Plus.

In addition to polymers having acetoacetyl functionality, coatingcompositions of the present invention also include ethylenicallyunsaturated compounds that are distinct from the acetoacetyl-functionalpolymers. Such compounds may be monomers, oligomers, polymers, ormixtures thereof. Preferred such ethylenically unsaturated compoundsinclude (meth)acrylate functionality (wherein “(meth)acrylate” refers toan acrylate and a methacrylate), vinyl ether functionality, (meth)allylether functionality (wherein (meth)allyl ether refers to an allyl etherand a methallyl ether), or mixtures thereof. Preferably, theethylenically unsaturated compound includes (meth)acrylatefunctionality. Examples of (meth)acrylate-functional compounds includethose selected from the group consisting of isobornyl (meth)acrylate,isodecyl (meth)acrylate, phenoxyethyl (meth)acrylate, trimethylolpropanetri(meth)acrylate, trimethylolpropane ethoxylate tri(meth)acrylate,tripropylene glycol di(meth)acrylate, hexanediol di(meth)acrylate,tetrahydrofurfuryl (meth)acrylate, beta-carboxyethyl (meth)acrylate,bisphenol A ethoxylate di(meth)acrylate, ethoxylated and propoxylatedneopentyl glycol di(meth)acrylates, di-(trimethyolpropane tetra(meth)acrylate), pentaerythritol tri(meth)acrylate, pentaerythritoltetra(meth)acrylate, and mixtures thereof.

The present invention also provides methods for coating that involveapplying a coating composition to a substrate and allowing the coatingcomposition to harden (e.g., by exposing the coating composition toradiation such as ultraviolet or visible light).

In one embodiment, a preferred method includes: providing a coatingcomposition that includes: water; a polymer that includes one or moreacetoacetyl-functional groups of the formula:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup; and a (meth)acrylate functional compound distinct from thepolymer having acetoacetyl functionality; optionally an initiator(preferably a photoinitiator); applying the coating composition to asubstrate surface; and at least partially curing the coatingcomposition.

In another embodiment, the method includes: providing a coatingcomposition that includes: water; a polymer including one or moreacetoacetyl-functional groups of the formula:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup; and an ethylenically unsaturated compound distinct from thepolymer having acetoacetyl functionality; a photoinitiator; applying thecoating composition to a substrate surface; and applying ultraviolet orvisible light to the coating composition to at least partially cure thecoating composition.

The present invention also provides coatings prepared or preparable fromthe coating compositions described herein. For example, a coating of thepresent invention is preparable by a method that involves applying acoating composition of the present invention to a substrate and allowingthe coating composition to harden (e.g., by exposing the coatingcomposition to radiation such as ultraviolet or visible light).

Preferred coatings are cured by exposing the coating to radiation havinga wavelength in the range of 10⁻³ to about 800 nm. More preferably,coating compositions of the present invention are exposed to ultravioletor visible light in the range of about 200 nm to 800 nm. Coatingcompositions of this invention may also be cured by thermal means orother forms of radiation such as, for example, electron beam.

Preferred coatings, which are designed to be cured by ultraviolet orvisible light, are preferably exposed to 100 Mjoules/cm² to 5000Mjoules/cm², more preferably exposed to 300 Mjoules/cm² to 2000Mjoules/cm², and even more preferably exposed to 500 Mjoules/cm² to 1750Mjoules/cm².

As used here, a “latex” polymer means a dispersion of polymer particlesin water; a latex polymer typically requires a secondary dispersingagent (e.g., a surfactant) for creating a dispersion or emulsion ofpolymer particles in water.

A “water-dispersible” polymer means the polymer is itself capable ofbeing dispersed into water (i.e., without requiring the use of aseparate surfactant) or water can be added to the polymer to form astable aqueous dispersion (i.e., the dispersion should have at least onemonth shelf stability at normal storage temperatures). Suchwater-dispersible polymers can include nonionic or anionic functionalityon the polymer, which assist in rendering them water-dispersible. Forsuch polymers, external acids or bases are typically required foranionic stabilization.

Also herein, “a,” “an,” “the,” “at least one,” and “one or more” areused interchangeably.

Also herein, the recitations of numerical ranges by endpoints includeall numbers subsumed within that range (e.g., 1 to 5 includes 1, 1.5, 2,2.75, 3, 3.80, 4, 5, etc.).

Also herein, the terms “comprises” and variations thereof do not have alimiting meaning where these terms appear in the description and claims.Thus, a composition comprising an ethylenically unsaturated compoundmeans that the composition includes one or more of the ethylenicallyunsaturated compounds.

The words “preferred” and “preferably” refer to embodiments of theinvention that may afford certain benefits, under certain circumstances.However, other embodiments may also be preferred, under the same orother circumstances. Furthermore, the recitation of one or morepreferred embodiments does not imply that other embodiments are notuseful, and is not intended to exclude other embodiments from the scopeof the invention.

The above summary of the present invention is not intended to describeeach disclosed embodiment or every implementation of the presentinvention. The description that follows more particularly exemplifiesillustrative embodiments. In several places throughout the application,guidance is provided through lists of examples, which examples can beused in various combinations. In each instance, the recited list servesonly as a representative group and should not be interpreted as anexclusive list.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

The present invention is directed to aqueous coating compositions (e.g.,paints) that include acetoacetyl functional polymers and ethylenicallyunsaturated compounds (monomers, oligomers, polymers, or mixturesthereof), coatings prepared therefrom, and methods of making and using.In some embodiments, the ethylenically unsaturated compounds are(meth)acrylate functional compounds.

Such polymers include one or more of the followingacetoacetyl-functional groups:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup. Preferably, R¹ is a C1 to C4 alkylene group and R² is a C1 to C4alkyl group, and more preferably, R¹ is methylene (—CH₂—) and R² ismethyl (—CH₃).

The amount of acetoacetyl functionality in such a polymer is preferablyat least 0.5%, more preferably at least 2.5%, and most preferably atleast 5%. The amount of acetoacetyl functionality in such a polymer ispreferably no more than 60%, more preferably no more than 40%, and mostpreferably no more than 30%.

In certain embodiments the invention relates to a radiation-curablecoating composition. More particularly, in certain preferredembodiments, the invention relates to an aqueous-based, ultraviolet(“UV”) radiation-curable coating composition containing anacetoacetyl-functional polymer and an acrylate or methacrylatefunctional (preferably, multifunctional) compound. Such coatings canalso be cured via visible light, electron beam, thermal initiation, orcationic initiation.

In certain embodiments the invention relates to an ultraviolet curablecoating composition. More particularly, in certain preferredembodiments, the invention relates to an aqueous-based, ultraviolet(“UV”) radiation-curable coating composition containing anacetoacetyl-functional polymer, an ethylenically unsaturated functionalcompound, and a photoinitiator.

In certain embodiments, coating compositions of the present inventionare advantageous in that they have a relatively low volatile organiccontent without sacrificing the balance of properties desired for anapplied (i.e., dry) coating, such as a paint. Preferably, certaincoating compositions have a relatively low volatile organic content(VOC). Preferably, the coating compositions include no more than 10weight percent (wt-%) volatile organic compounds, based on the totalweight of the composition. More preferably, the coating compositions ofthe present invention include no more than 7 wt-% volatile organiccompounds. Volatile organic compounds are defined in U.S. Pat. No.6,048,471 (Henry) and in the U.S. Federal Register: Jun. 16, 1995,volume 60, number 111.

Coating compositions of the present invention preferably include atleast 40 wt-% water, based on the total weight of the composition.Coating compositions of the present invention preferably include no morethan 90 wt-% water, and more preferably no more than 70 wt-% water,based on the total weight of the composition.

Polymers suitable for the coating compositions of the present inventionare preferably either water-dispersible or latex polymers. Such polymersare well-known in the coating industry and include a wide variety ofpolymers.

In certain embodiments, suitable polymers include polyurethanes,epoxies, polyamides, chlorinated polyolefins, acrylics, oil-modifiedpolymers, polyesters, and mixtures or copolymers thereof, for example.Such polymers are readily synthesized and made to include acetoacetylfunctionality using conventional techniques.

Acetoacetyl functionality may be incorporated into the polymer throughthe use of: acetoacetoxyethyl acrylate, acetoacetoxypropyl methacrylate,allyl acetoacetate, acetoacetoxybutyl methacrylate,2,3-di(acetoacetoxy)propyl methacrylate, 2-(acetoacetoxy) ethylmethacrylate, t-butyl acetoacetate, diketene, and the like, orcombinations thereof. In general, any polymerizable hydroxy functionalor other active hydrogen containing monomer can be converted to thecorresponding acetoacetyl functional monomer by reaction with diketeneor other suitable acetoacetylating agent (see, e.g., Comparison ofMethods for the Preparation of Acetoacetylated Coating Resins, Witzeman,J. S.; Dell Nottingham, W.; Del Rector, F. J. Coatings Technology; Vol.62, 1990, 101 (and references contained therein)). In preferred coatingcompositions, the acetoacetyl functional group is incorporated into thepolymer via 2-(acetoacetoxy) ethyl methacrylate, t-butyl acetoacetate,diketene, or combinations thereof.

In certain embodiments, the acetoacetyl-functional polymer of thecomposition is a latex polymer. Preferably, the acetoacetyl-functionallatex polymer particles have an average particle size of less than 75nanometers (nm).

In certain embodiments, the acetoacetyl functional latex polymer ispreferably prepared through chain-growth polymerization, using, forexample, 2-(acetoacetoxy) ethylmethacrylate (AAEM) and one or moreethylenically unsaturated monomers. Examples of ethylenicallyunsaturated monomers are selected from the group consisting of acrylicacid, methacrylic acid, methyl acrylate, ethyl acrylate, propylacrylate, butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate,ethyl methacrylate, propyl methacrylate, butyl methacrylate,2-ethylhexyl methacrylate, hydroxyethyl acrylate, hydroxyethylmethacrylate, hydroxybutyl acrylate, hydroxybutyl methacrylate, glycidylmethacrylate, 4-hydroxybutyl acrylate glycidylether, acrylamide,methylacrylamide, styrene, α-methyl styrene, vinyl toluene, vinylacetate, vinyl propionate, allyl methacrylate, and mixtures thereof.

Preferably, the ethylenically unsaturated monomers used in preparing theacetoacetyl-functional latex polymer include styrene. In certainembodiments, the acetoacetyl-functional latex polymer includes nogreater than 75 percent by weight (wt-%) styrene, and in otherembodiments, no greater than 50 wt-%, based on the total weight of theacetoacetyl-functional latex polymer. In certain embodiments, the levelof styrene is no less than 7.5 wt-%, in other embodiments, no less than20 wt-%, based on the total weight of the acetoacetyl-functional latexpolymer.

The latex polymers are typically stabilized by one or more nonionic oranionic emulsifiers (i.e., surfactants), used either alone or together.Examples of suitable nonionic emulsifiers includetert-octylphenoxyethylpoly(39)-ethoxyethanol,dodecyloxypoly(10)ethoxyethanol,nonylphenoxyethyl-poly(40)ethoxyethanol, polyethylene glycol 2000monooleate, ethoxylated castor oil, fluorinated alkyl esters andalkoxylates, polyoxyethylene (20) sorbitan monolaurate, sucrosemonococoate, di(2-butyl)phenoxypoly(20)ethoxyethanol,hydroxyethylcellulosepolybutyl acrylate graft copolymer, dimethylsilicone polyalkylene oxide graft copolymer, poly(ethyleneoxide)poly(butyl acrylate) block copolymer, block copolymers ofpropylene oxide and ethylene oxide,2,4,7,9-tetramethyl-5-decyne-4,7-diol ethoxylated with 30 moles ofethylene oxide, N-polyoxyethylene(20)lauramide,N-lauryl-N-polyoxyethylene(3)amine, and poly(10)ethylene glycol dodecylthioether. Examples of suitable anionic emulsifiers include sodiumlauryl sulfate, sodium dodecylbenzenesulfonate, potassium stearate,sodium dioctyl sulfosuccinate, sodium dodecyldiphenyloxide disulfonate,nonylphenoxyethylpoly(1)ethoxyethyl sulfate ammonium salt, sodiumstyrene sulfonate, sodium dodecyl allyl sulfosuccinate, linseed oilfatty acid, sodium or ammonium salts of phosphate esters of ethoxylatednonylphenol, sodium octoxynol-3-sulfonate, sodium cocoyl sarcocinate,sodium 1-alkoxy-2-hydroxypropyl sulfonate, sodium alpha-olefin (C₁₄-C₁₆)sulfonate, sulfates of hydroxyalkanols, tetrasodium N-(1,2-dicarboxyethyl)-N-octadecylsulfosuccinamate, disodiumN-octadecylsulfosuccinamate, disodium alkylamido polyethoxysulfosuccinate, disodium ethoxylated nonylphenol half ester ofsulfosuccinic acid and the sodium salt oftert-octylphenoxyethoxypoly(39)ethoxyethyl sulfate. Various combinationsof emulsifiers can be used, if desired.

The latex polymer may also be stabilized with an alkali-soluble polymer.Alkali-soluble polymers may be prepared by making a polymer with acrylicor methacrylic acid or other polymerizable acid monomer (usually greaterthan 10%) and solubilizing the polymer by addition of ammonia or otherbase. The alkali-soluble polymer may contain acetoacetyl functionality.Examples of suitable alkali-soluble support polymers are JONCRYL 675 andJONCRYL 678.

A water-soluble free radical initiator is typically used in the chaingrowth polymerization of a latex polymer. Suitable water-soluble freeradical initiators include hydrogen peroxide, tert-butyl peroxide,alkali metal persulfates such as sodium, potassium and lithiumpersulfate, ammonium persulfate, and mixtures of such initiators with areducing agent. Reducing agents include sulfites, such as alkali metalmetabisulfite, hydrosulfite, and hyposulfite, sodium formaldehydesulfoxylate, and reducing sugars such as ascorbic acid and isoascorbicacid. The amount of initiator is preferably from 0.01 wt-% to 3 wt-%,based on the total amount of monomer. In a redox system the amount ofreducing agent is preferably from 0.01 wt-% to 3 wt-%, based on thetotal amount of monomer. The temperature may be in the range of 10° C.to 100° C.

In certain embodiments, the acetoacetyl-functional polymer of thecomposition is a water dispersible polymer. Preferredacetoacetyl-functional water dispersible polymers include alkyds,polyesters, and polyurethanes. Such polymers may be prepared by anymethod known in the art.

An example of a method of preparing a water-dispersible polyesterincludes reacting one or more polybasic acids with one or more polyolsto give a polymer with excess hydroxyl functionality. The resultingpolyester could be further reacted with either t-butyl acetoacetate, ordiketene to incorporate acetoacetyl-functionality onto the polymer, andwith a suitable anhydride such as trimellitic anhydride to render thepolyester acid functional. The resulting acid functionality may then beneutralized with a neutralizing base to render the polyester waterdispersible.

An example of a method of preparing a water-dispersible alkyd includesreacting one or more of the alcoholysis product of an oil and polyol,fatty acids, monoglycerides or diglycerides and one or more polybasicacids with one or more polyols to give a polymer with excess hydroxylfunctionality. The resulting alkyd could be further reacted with eithert-butyl acetoacetate, or diketene to incorporateacetoacetyl-functionality onto the polymer, and with a suitableanhydride such as trimellitic anhydride to render the alkyd acidfunctional. The resulting acid functionality may then be neutralizedwith a neutralizing base to render the alkyd water dispersible.

Suitable oils and/or fatty acids derived therefrom include compoundssuch as, for example, linseed oil, safflower oil, tall oil, cotton seed,ground nut oil, tung oil, wood oil, ricinene oil or, preferably,sunflower oil, soya oil, castor oil, dehydrated castor oil, and thelike. These oils or fatty acids can be used alone or as a mixture of oneor more of the oils or fatty acids. Preferred fatty acids are soya fattyacids, dehydrated castor fatty acids, linolenic fatty acids, ricinoleicfatty acids, and linoleic fatty acids.

Suitable polyols useful in preparing a polyester or alkyd includecompounds such as, for example, aliphatic, cycloaliphatic and/oraraliphatic alcohols having 1 to 6, preferably 1 to 4, hydroxy groupsattached to nonaromatic or aromatic carbon atoms. Examples of suitablepolyols include, ethylene glycol, 1,2-propanediol, 1,3-propanediol,1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 2-ethyl-1,3-propanediol,2-methylpropanediol, 2-butyl2-ethylpropanediol, 2-ethyl-1,3-hexanediol,1,3 neopentyl glycol, 2,2-dimethyl-1,3-pentanediol, 1,6 hexanediol, 1,2-and 1,4-cyclohexanediol, bisphenol A, 1,2- and1,4-bis(hydroxymethyl)cyclohexane, bis(4-hydroxycyclohexyl)-methane,adipic acid bis-(ethylene glycol ester), ether alcohols, such asdiethylene glycol and triethylene glycol, dipropylene glycol,perhydrogenated bisphenols, 1,2,4-butanetriol, 1,2,6-hexanetriol,trimethylolethane, trimethylolpropane, trimethylolhexane, glycerol,pentaerythritol, dipentaerythritol, mannitol and sorbitol, and alsochain-terminating monoalcohols having 1 to 8 carbon atoms such aspropanol, butanol, cyclohexanol, benzyl alcohol, hydroxypivalic acid,and mixtures thereof.

The polybasic acids useful in preparing polyesters or alkyds includecompounds such as, for example, aliphatic, cycloaliphatic saturated orunsaturated and/or aromatic polybasic carboxylic acids, such as, forexample, dicarboxylic, tricarboxylic and tetracarboxylic acids. Thesecompounds can be used alone or as a mixture of one or more polybasicacids. Suitable examples of polybasic acids include, for example,phthalic acid, isophthalic acid, adipic acid, terephthalic acid,tetrahydrophthalic acid, hexahydrophthalic acid,endomethylenetetrahydrophthalic acid, succinic acid, glutaric acid,sebacic acid, azelaic acid, trimellitic acid, pyromellitic acid, fumaricand maleic acid and the like, or mixtures thereof.

Polybasic acids, as used herein, are broadly defined to includeanhydrides of the polybasic acids such as, for example, maleicanhydride, phthalic anhydride, succinic anhydride, tetrahydrophthalicanhydride, hexahydrophthalic anhydride, trimellitic anhydride, ormixtures thereof. These compounds can be used alone or as a mixture ofone or more polybasic acids.

Suitable neutralizing bases to render the polyester or alkyd waterdispersible include inorganic bases such as sodium hydroxide, potassiumhydroxide, lithium hydroxide, ammonia, triethylamine, and dimethylethanol amine.

In addition to polymers having acetoacetyl functionality, coatingcompositions of the present invention also include ethylenicallyunsaturated compounds. Preferably, such compounds are multifunctional(i.e., include two or more ethylenically unsaturated groups), whichmakes them suitable crosslinkable diluents. Such compounds may bemonomers, oligomers, polymers, or mixtures thereof.

Preferred such ethylenically unsaturated compounds include(meth)acrylate functionality (wherein “(meth)acrylate” refers to anacrylate and a methacrylate), vinyl functionality, vinyl etherfunctionality, (meth)allyl ether functionality (wherein (meth)allylether refers to an allyl ether and a methallyl ether), or mixturesthereof.

Coating compositions of the present invention can include one or moredifferent ethylenically unsaturated compounds, preferably one or more(meth)acrylate monomers. Preferably, the (meth)acrylate monomers havetwo or more (meth)acrylate groups (i.e., they are multifunctional). The(meth)acrylate functional groups of the (meth)acrylate monomers arebonded to core structural groups, which may be based on a wide varietyof organic structures including tripropylene glycol, isobornyl alcohol,isodecyl alcohol, phenoxyethyl alcohol, trishydroxyethyl isocyanurate,trimethylolpropane ethoxylate, hexanediol, ethoxylated and propoxylatedneopentyl glycol, oxyethylated phenol, polyethylene glycol, bisphenolethoxylate, neopentyl glycol propoxylate, trimethylolpropane,propoxylated glycerol, di-trimethylolpropane, pentaerythritol,tetrahydrofurfuryl alcohol, beta-carboxyethyl alcohol, substitutedderivatives of the above, combinations of the above, and the like.

Examples of suitable (meth)acrylate monomers include isobornyl(meth)acrylate, isodecyl (meth)acrylate, phenoxyethyl (meth)acrylate,trimethylolpropane tri(meth)acrylate, trimethylolpropane ethoxylatetri(meth)acrylate, tripropylene glycol di(meth)acrylate, hexanedioldi(meth)acrylate, tetrahydrofurfuryl (meth)acrylate, beta-carboxyethyl(meth)acrylate, bisphenol A ethoxylate di(meth)acrylate, ethoxylated andpropoxylated neopentyl glycol di(meth)acrylates, di-(trimethyolpropanetetra (meth)acrylate), pentaerythritol tri(meth)acrylate,pentaerythritol tetra(meth)acrylate, or mixtures thereof.

Another example of a suitable ethylenically unsaturated compound is anallyl ether. Preferably, the allyl ether functional groups of the allylether monomers are bonded to a core structural group which is based on awide variety of polyhydric alcohols. Suitable polyhydric alcoholsinclude neopentyl glycol, trimethylolpropane, ethylene glycol, propyleneglycol, butylene glycol, diethylene glycol, trimethylene glycol,triethylene glycol, trimethylolethane, pentaerythritol, glycerol,diglycerol, 1,4-butanediol, 1,6-hexanediol, 1,4-cyclohexanedimethanol,and the like. Various mixtures of such alcohols can be used, if desired.

Examples of suitable allyl ether monomers include hydroxyethyl allylether, hydroxypropyl allyl ether, trimethylolpropane monoallyl ether,trimethylolpropane diallyl ether, trimethylolethane monoallyl ether,trimethylolethane diallyl ether, glycerol monoallyl ether, glyceroldiallyl ether, pentaerythritol monoallyl ether, pentaerythritol diallylether, pentaerythritol triallyl ether, 1,2,6-hexanetriol monoallylether, 1,2,6-hexanetriol diallyl ether, and the like. Propoxylated andethoxylated forms of these compounds are also suitable.

Another example of a suitable ethylenically unsaturated compound is avinyl ether. Examples of suitable vinyl ether monomers include4-hydroxybutyl vinyl ether, 1,4-cyclohexanedimethanol monovinyl ether,1,4-cyclohexanedimethanol divinyl ether, ethylene glycol monovinylether, ethylene glycol divinyl ether, diethylene glycol monovinyl ether,diethylene glycol divinyl ether, triethylene glycol divinyl ether, andthe like. Propoxylated and ethoxylated forms of these compounds are alsosuitable.

The ethylenically unsaturated compounds may be used in variouscombinations and may also provide a crosslinkable diluent function tothe coating compositions.

Coating compositions of the present invention preferably include anacetoacetyl-functional polymer in an amount of at least 30 wt-%, morepreferably at least 45 wt-%, and even more preferably at least 55 wt-%,based on the combined weight of the ethylenically unsaturated compoundand the acetoacetyl-functional polymer component of the composition.Coating compositions of the present invention preferably include anacetoacetyl-functional polymer in an amount of no more than 95 wt-%,more preferably no more than 90 wt-%, and even more preferably no morethan 85 wt-%, based on the combined weight of the ethylenicallyunsaturated compound and the acetoacetyl-functional polymer component ofthe composition.

Thus, certain preferred coating compositions include 30 wt-% to 95 wt-%acetoacetyl-functional polymer, and in certain more preferredcompositions include 55 wt-% to 85 wt-% acetoacetyl-functional polymer,based on the combined weight of the ethylenically unsaturated compoundand the acetoacetyl-functional polymer component of the composition.

Coating compositions of the present invention preferably include anethylenically unsaturated compound in an amount of at least 5 wt-%, morepreferably in an amount of at least 7.5 wt-%, and even more preferablyin an amount of at least 10 wt-%, based on the combined weight of theethylenically unsaturated compound and the acetoacetyl-functionalpolymer component of the composition. Coating compositions of thepresent invention preferably include an ethylenically unsaturatedcompound in an amount of no more than 70 wt-%, more preferably in anamount of no more than 50 wt-%, and even more preferably in an amount ofno more than 40 wt-%, based on the combined weight of the ethylenicallyunsaturated compound and the acetoacetyl-functional polymer component ofthe composition.

Other components of the coating compositions of the present inventioninclude those typically used in paint formulations, such as pigments,fillers, thickeners, biocides, mildewcides, surfactants, dispersants,defoamers, and the like. Suitable additives for use in coatingcompositions of the present invention are described in Koleske et al.,Paint and Coatings Industry, April, 2003, pages 12-86.

In particular, compositions including a latex polymer also include adispersing agent, such as a nonionic or anionic surfactant, as describedabove. Such surfactants not only create a dispersion or emulsion ofpolymer particles in water, but assist incorporation of theethylenically unsaturated compound.

Coating compositions of the present invention can include one or moreinitiators. Examples of suitable initiators include photoinitiators,thermal initiators, catalysts for auto-oxidative cure (e.g., manganesecatalysts).

Certain embodiments of the present invention include polymers that arecurable by UV or visible light. These coating compositions typicallyinclude a free-radical initiator, particularly a photoinitiator thatinduces the curing reaction upon exposure to light. The photoinitiatoris preferably present in an amount of at least 0.1 wt-%, based on thetotal weight of the coating composition. The photoinitiator ispreferably present in an amount of no greater than 10 wt-%, based on thetotal weight of the coating composition.

Among photoinitiators suitable for use in the present invention withresins having (meth)acrylate or allyl ether functional groups arealpha-cleavage type photoinitiators and hydrogen abstraction-typephotoinitiators. The photoinitiator may include other agents such as acoinitiator or photoinitiator synergist that aid the photochemicalinitiation reaction. Suitable cleavage type photoinitiators includealpha, alpha-diethoxyacetophenone (DEAP), dimethoxyphenylacetophenone(commercially available under the trade designation IRGACURE 651 fromCiba Corp., Ardsley, N.Y.), hydroxycyclo-hexylphenylketone (commerciallyavailable under the trade designation IRGACURE 184 from Ciba Corp.),2-hydroxy-2-methyl-1-phenylpropan-1-one (commercially available underthe trade designation DAROCUR 1173 from Ciba Corp.), a 25:75 blend ofbis-(2,6-dimethoxybenzoyl)-2,4,4-trimethylpentyl phosphine oxide and2-hydroxy-2-methyl-1-phenylpropan-1-one (commercially available underthe trade designation IRGACURE 1700 from Ciba Corp.), a 50:50 blend of2-hydroxy-2-methyl-1-phenylpropan-1-one and2,4,6-trimethylbenzoyl-diphenylphosphine oxide (TPO, commerciallyavailable under the trade designation DAROCUR 4265 from Ciba Corp.),phosphine oxide, 2,4,6-trimethyl benzoyl (commercially available underthe trade name IRGACURE 819 and IRGACURE 819DW from Ciba Corp.),2,4,6-trimethylbenzoyl-diphenylphosphine oxide (commercially availableunder the trade designation LUCIRIN from BASF Corp., Mount Olive, N.J.),and a mixture of 70% oligo2-hydroxy-2-methyl-4-(1-methylvinyl)phenylpropan-1-one and 30%2-hydroxy-2-methyl-1-phenylpropan-1-one) (commercially available underthe trade designation KIP 100 from Sartomer, Exton, Pa.). Suitablehydrogen abstraction-type photoinitiators include benzophenone,substituted benzophenones (such as that commercially available under thetrade designation ESCACURE TZT from Fratelli-Lamberti, sold by Sartomer,Exton, Pa.), and other diaryl ketones such as xanthones, thioxanthones,Michler's ketone, benzil, quinones, and substituted derivatives of allof the above. Preferred photoinitiators include DAROCUR 1173, KIP 100,benzophenone, and IRGACURE 184. A particularly preferred initiatormixture is commercially available under the trade designation IRGACURE500 from Ciba Corp., which is a mixture of IRGACURE 184 andbenzophenone, in a 1:1 ratio. This is a good example of a mixture of analpha-cleavage type photoinitiator and a hydrogen abstraction-typephotoinitiator. Other mixtures of photoinitiators may also be used inthe coating compositions of the present invention. Camphorquinone is oneexample of a suitable photoinitiator for curing a coating compositionwith visible light.

A coating composition of the present invention can also include acoinitiator or photoinitiator synergist. The coinitiators can betertiary aliphatic amines (such as methyl diethanol amine and triethanolamine), aromatic amines (such as amylparadimethylaminobenzoate,2-n-butoxyethyl-4-(dimethylamino) benzoate,2-(dimethylamino)ethylbenzoate, ethyl-4-(dimethylamino)benzoate, and2-ethylhexyl-4-(dimethylamino)benzoate, (meth)acrylated amines (such asthose commercially available under the trade designations EBECRYL 7100and UVECRYL P104 and P115, all from UCB RadCure Specialties, Smyrna,Ga.), and amino-functional acrylate or methacrylate resin or oligomerblends (such as those commercially available under the tradedesignations EBECRYL 3600 or EBECRYL 3703, both from UCB RadCureSpecialties). Combinations of the above categories of compounds may alsobe used.

Preferred photoinitiators include benzophenone, 4-methylbenzophenone,benzoyl benzoate, phenylacetophenones,2,2-dimethoxy-2-phenylacetophenone, alpha,alpha-diethoxyacetophenone,hydroxycyclo-hexylphenylketone, 2-hydroxy-2-methyl-1-phenylpropan-1-one,bis-(2,6-dimethoxybenzoyl)-2,4,4-trimethylpentyl phosphine oxide,2-hydroxy-2-methyl-1-phenylpropan-1-one,2-hydroxy-2-methyl-1-phenylpropan-1-one,2,4,6-trimethylbenzoyl-diphenylphosphine oxide, and combinationsthereof.

Preferred compositions include a free radical initiator that is ahydrogen abstraction-type photoinitiator. Preferably, the hydrogenabstraction-type photoinitiator is benzophenone or a4-methylbenzophenone. Such compositions are at least partially curableby ultraviolet light.

Although not intended to be limiting, it is believed that theacetoacetyl-functional polymer likely participates in a free radical UVcure mechanism through hydrogen abstraction of the —C(O)—CH₂—C(O)—hydrogens through a benzophenone based initiation. If it occurs, thispreferably takes place upon exposure to ultraviolet or visible lightbetween 200 nm and 800 nm, and more preferably in the ultraviolet rangeof 200 nm to 400 nm.

The amount of hydrogen abstraction-type photoinitiator in such acomposition is preferably at least 0.1 wt-%, more preferably at least0.2 wt-%, and even more preferably at least 0.4 wt-%, based upon thetotal weight of the composition. The amount of hydrogen abstraction-typephotoinitiator in such a composition is preferably no more than 4 wt-%,more preferably no more than 3 wt-%, and even more preferably no morethan 2 wt-%, based upon the total weight of the composition.

Coating compositions having resins with vinyl ether functional groupscan be cured by UV or visible light using cationic-generatingphotoinitiators. Examples of suitable cationic-generatingphotoinitiators include super acid-generating photoinitiators, such astriarylsulfonium salts. One useful triarylsulfonium salt is triphenylsulfonium hexafluorophosphate.

Many coating compositions that may be cured by UV or visible light mayalso be cured with an electron beam. Techniques and devices for curing acoating composition using an electron beam are known in the art. Thesetechniques do not require a photoinitiator for electron beam cure of thecoating.

Coating compositions that include compounds with (meth)acrylate and/orallyl functional groups may also be thermally cured using a suitableinitiator. The thermal initiator typically facilitates the curingprocess by a free radical mechanism and typically includes a peroxide orazo compound. Peroxide compounds suitable for use as initiators in thecoating compositions of the present invention include t-butylperbenzoate, t-amyl perbenzoate, cumene hydroperoxide, t-amylperoctoate, methyl ethyl ketone peroxide, benzoyl peroxide,cyclohexanone peroxide, 2,4-pentanedione peroxide, di-t-butyl peroxide,t-butyl hydroperoxide, and di-(2-ethylhexyl)-peroxydicarbonate. Suitableazo compounds which may be employed as an initiator in the presentcompositions include 2,2-azo bis-(2,4-dimethylpentane-nitrile), 2,2-azobis-(2-methylbutanenitrile), and 2,2-azo bis-(2-methylpropanenitrile).

For coating compositions having a mixture of (meth)acrylate, allylether, and vinyl ether functional groups, a combination of curingprocedures may be used. For example, a coating composition having both(meth)acrylate and vinyl ether functional groups typically includes analpha-cleavage type and/or hydrogen abstraction type photoinitiator forthe (meth)acrylate groups and a cationic-generating photoinitiator forthe vinyl ether groups.

Other methods for curing the coating compositions of the invention canbe used alone or in combination with methods described hereinabove.Supplemental curing methods include heat cure, chemical cure, anaerobiccure, moisture cure, oxidative cure, and the like. Each method of curerequires a corresponding curing initiator or curing agent, which isincluded in the composition. For example, thermal cure can be induced byperoxides, metal drier packages can induce an oxidative cure,multifunctional amines (for example isophorone diamine) can effect achemical crosslinking cure through Michael addition of amine groups ontoacrylate reactive unsaturated groups. If these additional initiators arepresent in the coating composition they are preferably present in anamount of at least 0.1 wt-%, based on the weight of the coatingcomposition. Preferably, they are present in an amount of no greaterthan 12 wt-%, based on the weight of the coating composition. Means foreffecting cures by such methods are known to those of skill in the artor can be determined using standard methods.

Certain coating compositions of the present invention may also includeone or more of a group of ingredients that can be called performanceenhancing additives. Typical performance enhancing additives that may beemployed include surface active agents, pigments, colorants, dyes,surfactants, thickeners, heat stabilizers, leveling agents,anti-cratering agents, curing indicators, plasticizers, fillers,sedimentation inhibitors, ultraviolet-light absorbers, opticalbrighteners, and the like to modify properties.

Coating compositions may include a surface-active agent that modifiesthe interaction of the curable coating composition with the substrate,in particular, the agent can modify the ability of the composition towet a substrate. Surface active agents may have other properties aswell. For example, surface active agents may also include leveling,defoaming, or flow agents, and the like. The surface active agentaffects qualities of the curable coating composition including how thecoating composition is handled, how it spreads across the surface of thesubstrate, and how it bonds to the substrate. If it is used, the surfaceactive agent is preferably present in an amount of no greater than 5wt-%, based on the total weight of the coating composition.

Surface active agents have also been found to assist incorporation aswell as assist coating formulation. Surface active agents suitable foruse in coating compositions are known to those of skill in the art orcan be determined using standard methods. Exemplary surface activeagents include polydimethylsiloxane surface active agents (such as thosecommercially available under the trade designations SILWET L-760 andSILWET L-7622 from OSI Specialties, South Charleston, W. Va., or BYK306, BYK 333, and BYK 346 from Byk-Chemie, Wallingford, Conn.) andfluorinated surface active agents (such as that commercially availableas FLUORAD FC-430 from 3M Co., St. Paul, Minn.). The surface activeagents may include a defoamer. Suitable defoamers include polysiloxanedefoamers (such as a methylalkylpolysiloxane like that commerciallyavailable under the trade designation BYK 077 or BYK 500 fromByk-Chemie) or polymeric defoamers (such as that commercially availableunder the trade designation BYK 051 from Byk-Chemie).

For some applications, a coating that is opaque, colored, pigmented orhas other visual characteristics is desired. Agents to provide suchproperties can also be included in coating compositions of the presentinvention. Pigments for use with the present invention are known in theart. Suitable pigments include titanium dioxide white, carbon black,lampblack, black iron oxide, red iron oxide, yellow iron oxide, browniron oxide (a blend of red and yellow oxide with black), phthalocyaninegreen, phthalocyanine blue, organic reds (such as naphthol red,quinacridone red and toulidine red), quinacridone magenta, quinacridoneviolet, DNA orange, and/or organic yellows (such as Hansa yellow). Thecomposition can also include a gloss control additive or an opticalbrightener, such as that commercially available under the tradedesignation UVITEX OB from Ciba-Geigy.

In certain embodiments it is advantageous to include fillers or inertingredients in the coating composition. Fillers and inert ingredientsinclude, for example, clay, glass beads, calcium carbonate, talc,silicas, organic fillers, and the like. Fillers extend, lower the costof, alter the appearance of, or provide desirable characteristics to thecomposition before and after curing. Suitable fillers are known to thoseof skill in the art or can be determined using standard methods. Fillersor inert ingredients are preferably present in an amount of at least 0.1wt-%, based on the total weight of the coating composition. Fillers orinert ingredients are preferably present in an amount of no greater than40 wt-%, based on the total weight of the coating composition.

The invention may also include other ingredients that modify propertiesof the curable coating composition as it is stored, handled, or applied,and at other or subsequent stages. Waxes, flatting agents, mar andabrasion additives, and other similar performance enhancing additivesmay be employed in this invention as required in amounts effective toupgrade the performance of the cured coating and the coatingcomposition. Desirable performance characteristics of the coatinginclude chemical resistance, abrasion resistance, hardness, gloss,reflectivity, appearance, or combinations of these characteristics, andother similar characteristics.

The coating compositions of the present invention may be applied to avariety of substrates including wood, cement, cement fiber board,wood-plastic composites, tile, metal, plastic, glass, optical fibers,and fiberglass. Coating compositions can be applied to a substrate by avariety of methods known to those skilled in the art. Such methodsinclude spraying, painting, rollcoating, brushing, fan coating, curtaincoating, spreading, air knife coating, die-coating, vacuum coating, spincoating, electrodeposition, and dipping.

The thickness of the coatings will vary with the application. Typically,the coatings will have a thickness of 0.1 mil to 20 mils (0.00025centimeter (cm) to 0.0508 cm), however, thicker or thinner coatings arealso contemplated depending on, for example, the desired coatingproperties.

The present invention also provides methods for coating that involveapplying a coating composition to a substrate and allowing the coatingcomposition to harden (e.g., by exposing the coating composition toradiation such as ultraviolet or visible light). The present inventionalso provides coatings prepared or preparable from the coatingcompositions described herein. For example, a coating of the presentinvention is preparable by a method that involves applying a coatingcomposition of the present invention to a substrate and allowing thecoating composition to harden (e.g., by exposing the coating compositionto radiation such as ultraviolet or visible light).

Preferred coatings are cured by exposing the coating to radiation havinga wavelength in the range of 10⁻³ nm to 800 nm. More preferably, coatingcompositions of the present invention are exposed to ultraviolet orvisible light in the range of 200 nm to 800 nm. Coating compositions ofthis invention may also be cured by thermal means or other forms ofradiation such as, for example, electron beam.

Preferred coatings, which are designed to be cured by ultraviolet orvisible light, are preferably exposed to 100 Mjoules/cm² to 5000Mjoules/cm², more preferably exposed to 300 Mjoules/cm² to 2000Mjoules/cm², and even more preferably exposed to 500 Mjoules/cm² to 1750Mjoules/cm².

A preferred method includes: providing a coating composition thatincludes: water; a polymer that includes one or moreacetoacetyl-functional groups of the formula:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup; and a (meth)acrylate functional compound distinct from thepolymer having acetoacetyl functionality; optionally an initiator(preferably a photoinitiator); applying the coating composition to asubstrate surface; and at least partially curing the coatingcomposition.

Another embodiment of the method includes: providing a coatingcomposition that includes: water; a polymer including one or moreacetoacetyl-functional groups of the formula:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup; and an ethylenically unsaturated compound distinct from thepolymer having acetoacetyl functionality; a photoinitiator; applying thecoating composition to a substrate surface; and applying ultraviolet orvisible light to the coating composition to at least partially cure thecoating composition.

EXAMPLES

The following examples are offered to aid in understanding of thepresent invention and are not to be construed as limiting the scopethereof. Unless otherwise indicated, all parts and percentages are byweight.

Reagents:

DMPA—Dimethylolpropionic acid (GEO, Allentown, Pa.)

TMPTA—Trimethylolpropane triacrylate (Sartomer, Exton, Pa.)

EOTMPTA—Ethoxylated trimethylol propane triacrylate (Sartomer, Exton,Pa.)

4-HBA—4-Hydroxy butylacrylate (Aldrich, Milwaukee, Wis.)

TMP—Trimethylol Propane (Aldrich)

DESMOPHEN S-105-110—Polyester diol (Bayer, Pittsburgh, Pa.)

TEA—Triethyl Amine (Aldrich)

DBTDL—Dibutyl Tin Dilaurate (Air Products, Allentown, Pa.)

RHODAPON UB—Sodium Lauryl Sulfate (Rhodia, Cranbury, N.J.)

RHODAPON UB—Sodium Lauryl Sulfate (Rhodia, Cranbury, N.J.)

RHODAPEX CO-436—Nonylphenol Ethoxylated, Sulfate, NH3 Salt (Rhodia,Cranbury, N.J.)

IPA—Isophthalic Acid (Amoco, Chicago, Ill.)

AA—Adipic Acid (Aldrich Chemical, Milwaukee, Wis.)

TMA—Trimellitic Anhydride (Aldrich Chemical, Milwaukee, Wis.)

NPG—Neopentyl Glycol (Aldrich Chemical, Milwaukee, Wis.)

DPG—Dipropylene Glycol (Aldrich Chemical, Milwaukee, Wis.)

AAEM—2-(acetoacetoxy) ethyl methacrylate (Aldrich Chemical, Milwaukee,Wis.)

t-BAcAc—t-butyl acetoacetate (Aldrich Chemical, Milwaukee, Wis.)

NMP—n-methylpyrrolidinone (Aldrich Chemical, Milwaukee, Wis.)

Example 1: Preparation of an Acetoacetyl-Functional Latex Polymer

A reactor is charged with 775.2 parts of deionized water and 18.4 partsCO-436. The reaction mixture is heated to 75° C. under a nitrogenblanket. During heating, a premulsion is formed comprising: 336.4 partsof deionized water, 12.2 parts CO-436, 0.8 parts ammonium persulfate,370.0 parts of butyl acrylate, 190.2 parts of methyl methacrylate, 118.3parts of styrene, 78.9 parts AAEM and 31.5 parts of methacrylic acid.Once the reaction mixture reaches 75° C., 5% of the preemulsion is addedto the reactor followed by the addition of a mixture of 2.4 parts ofammonium persulfate and 7.5 parts of water. The reaction is held 5-10minutes, whereupon an exotherm results and then the remainingpreemulsion is fed into the reactor vessel over 2 hours. The reactiontemperature is held between 80° C. and 85° C., during polymerization.Once the preemulsion feed is complete, the container is rinsed with 20parts of deionized water and the reaction is held 30 minutes. Once the30 minute hold is complete, the resulting latex polymer is cooled to 40°C. and a 28% concentrate ammonia is added to adjust the pH to 7.0-7.5and deionized water is added to adjust the weight solids to 40%.

Example 2: Preparation of a Ultraviolet Curable Acetoacetyl-FunctionalCoating Composition

Under agitation to a stainless steel mixing vessel is added 100 grams ofdeionized water, 14.2 grams of RHODAPAN UB, and 200 grams EOTMPTA. Themixture is blended until a pre-emulsion forms.

Under agitation to a stainless steel mixing vessel is added 1000 gramsof latex polymer from Example 1, 93 grams of deionized water, and 157grams of the EOTMPTA pre-emulsion prepared above. This mixture is thenheld under agitation for 8 hours until the EOTMPTA migrates into thelatex polymer. Fifteen (15) grams of IRGACURE 500 is then added to themixture and held under agitation for another 15 minutes. The mixture isthen left overnight to allow the release of any entrapped air.

The resulting mixture will cure to a hard, chemically resistant finishupon exposure to ultraviolet light. The resulting mixture from Example 2will also cure to a hard, chemically resistant finish without the needof photoinitiator under electron beam radiation.

Example 3: Preparation of (Meth)Acrylate Functional PolyurethaneDispersion (PUD) with TMPTA Reactive Diluent

A reactor is charged with 96.0 parts TMPTA, 48.0 parts 4-HBA, 91.4 partsDESMOPHEN S-105-110 polyester diol, 29.3 parts DMPA, 9.6 parts TMP,258.9 parts isophorone diisocyanate, and 500 ppm of 2,6di-tert-butyl-4-methylphenol. The reaction mixture is heated to 80° C.under an air sparge, where upon 250 ppm DBTDL is added and the reactionprocessed until the isocyanate level is below 9.2%. The urethane polymeris cooled to 65° C. and then neutralized with 22.1 parts TEA. Theurethane polymer viscosity at 65° C. will be less than 6,000 centipoise(cps) as measured by a Brookfield DV-I+ Viscometer and a Number 31spindle at 1.5 revolutions per minute (RPM).

At a process temperature of 65° C., the (meth)acrylate urethane polymerformed above is then dispersed into 895.5 parts room temperaturedeionized water and subsequently chain extended with 51.1 partshydrazine (35% in water). The dispersion is then adjusted to 35% solidswith deionized water.

The physical properties of the chain extended (meth)acrylate functionalpolyurethane dispersion are as follows (NVM %=nonvolatile material byweight):

EXAMPLE 1 NVM % 35% % VOC 1.4% (TEA)

Example 4: Preparation of a Ultraviolet Curable Acetoacetyl-FunctionalCoating Composition

Under agitation to a stainless steel mixing vessel is added 100 grams ofdeionized water, 14.2 grams of Rhodapon UB, and 200 grams EOTMPTA. Themixture is blended until a pre-emulsion forms.

Under agitation to a stainless steel mixing vessel is added 800 grams oflatex polymer from Example 1, 200 grams of the polymer from Example 3,93 grams of deionized water, and 157 grams of the EOTMPTA preemulsionprepared above. This mixture is then held under agitation for 8 hoursuntil the EOTMPTA migrates into the latex polymer. Fifteen (15) grams ofIRGACURE 500 is then added to the mixture and held under agitation foranother 15 minutes. The mixture is then left overnight to allow therelease of any entrapped air.

The resulting mixture will cure to a hard, chemically resistant finishupon exposure to ultraviolet light. The resulting mixture from Example 4will also cure to a hard, chemically resistant finish without the needof photo initiator under electron beam radiation.

Example 5: Preparation of Acetoacetyl-Functional Water DispersiblePolyester

A reactor is charged with 383.9 parts IPA, 135.5 parts AA, 383.9 partsDPG, 101.6 parts TMP and 1500 ppm of Fascat 4100 tin catalyst from ElfAtochem. The reaction mixture is slowly heated 235° C. and stirred forabout 4 hours and water is removed. The mixture is heated and testeduntil a sample has an acid number of less than 20 mg of KOH/gram. Atwhich point 79 parts t-BAcAc is added and held at 235° C. while removingmethanol. Once methanol stops coming off, the mixture is cooled to 200°C. and 45.2 parts TMA is added. The reaction is held at 190° C. andtested until the acid number is 40-45 mg of KOH/gram. Once the acidnumber is 40-45 mg of KOH/gram, the reaction is cooled to 100° C., andair sparge is begun and 1000 ppm MEHQ is added along with 333 gramsEOTMPTA. To this mixture is added 45 parts of 28% ammonia and 2400 partsdeionized water. As the water is added, the mixture is allowed to coolto room temperature and the solids are adjusted to 35%.

Example 6: Preparation of a Ultraviolet Curable Acetoacetyl-FunctionalCoating Composition

Fifteen (15) grams of IRGACURE 500 is added to 1500 grams of the mixturefrom Example 5 and held under agitation for another 15 minutes. Themixture is then left overnight to allow the release of any entrappedair.

The resulting mixture will cure to a hard, chemically resistant finishupon exposure to ultraviolet light. The resulting mixture from Example 6will also cure to a hard, chemically resistant finish without the needof photo initiator under electron beam radiation.

Example 7: Preparation of an Acetoacetyl-Functional Latex Polyer

A reactor was charged with 522.6 parts of deionized water, 1.8 partsRHODAPON UB. The reaction mixture was heated to 75° C. under a nitrogenblanket. During heating, a premulsion was formed comprising: 299.9 partsof deionized water, 57.4 parts of RHODAPON UB, 0.7 part ammoniumpersulfate, 156.6 parts of butyl acrylate, 176.0 parts of butylmethacrylate, 463.8 parts of styrene, 44.0 parts AAEM, and 39.6 parts ofmethacrylic acid. Once the reaction mixture reaches 75° C., 5% of thepreemulsion was added to the reactor followed by the addition of amixture of 2.0 parts of ammonium persulfate and 8.1 parts of water. Thereaction was held for 5 minutes to 10 minutes, whereupon an exothermresults and then the remaining pre-emulsion was fed into the reactorvessel over 2 hours. The reaction temperature was held between 80° C.and 85° C., during polymerization. Once the preemulsion feed wascomplete, the container was rinsed with 9 parts of deionized water andthe reaction was held 30 minutes. As the prepolymer became viscous, 100parts additional deionized water was added. Once the 30 minute hold wascomplete, the resulting latex polymer was cooled to 40° C. and a 28%concentrate ammonia was added to adjust the pH to 7.0-7.5 and deionizedwater was added to adjust the weight solids to 45%.

Example 8: Comparative Example—Preparation of a NonAcetoacetyl-Functional Latex Polymer

A reactor was charged with 521.9 parts of deionized water, 3.0 partsRHODAPON UB. The reaction mixture was heated to 75° C. under a nitrogenblanket. During heating, a premulsion was formed comprising: 300.5 partsof deionized water, 56.1 parts of RHODAPON UB, 0.7 pars ammoniumpersulfate, 179.7 parts of butyl acrylate, 176.0 parts of butylmethacrylate, 484.8 parts of styrene, and 39.6 parts of methacrylicacid. Once the reaction mixture reaches 75° C., 10% of the preemulsionwas added to the reactor followed by the addition of a mixture of 2.0parts of ammonium persulfate and 8.1 parts of water. The reaction washeld for 5 minutes to 10 minutes, whereupon an exotherm results and thenthe remaining preemulsion was fed into the reactor vessel over 2 hours.The reaction temperature was held between 80° C. to 85° C., duringpolymerization. Once the preemulsion feed was complete, the containerwas rinsed with 9 parts of deionized water and the reaction was held 30minutes. As the prepolymer became viscous, 30 parts additional deionizedwater was added. Once the 30 minute hold was complete, the resultinglatex polymer was cooled to 40° C. and a 28% concentrate ammonia wasadded to adjust the pH to 7.0-7.5 and deionized water was added toadjust the weight solids to 45%.

Example 9: Test Comparison of the Latex Polymers from Examples 7 and 8

The following compositions were prepared and allowed to mix for 8 hours.At which point 1% IRGACURE 500, based on the total weight of thecomposition, was added to each sample and the samples were allowed tosit overnight to release any trapped air.

Components COMPOSITION A COMPOSITION B Latex from Example 7 50 gramsLatex from Example 8 50 grams Water  6 grams  6 grams EOTMPTA  6 grams 6 grams NMP  1 gram  1 gramPhysical Testing

A 3-mil thick (0.00762-cm) wet film was then applied to a Leneta Form 7Btest chart and air dried for 15 minutes followed by force dry for 5minutes at 65° C. The dried (meth)acrylate polymer film was then curedby mercury ultraviolet lamps. Total UV exposure was 1000 millijoules persquare centimeter (mj/cm²).

Performance properties are outlined below. Gloss is reported inaccordance with ASTM test specification, D-523. All other cured filmproperties are reported on a scale of 1-10, with 10 being no effect orbest.

TEST COMPOSITION A COMPOSITION B MEK 2× Rubs >100 <100

MEK double rub testing was performed in accordance with ASTM test methodD-5402. Composition A only showed surface marring after 100 MEK doublerubs while composition B showed lower chemical resistance and showedfilm failure and breakthrough to the substrate at 100 double rubs.

Having thus described the preferred embodiments of the presentinvention, those skilled in the art will readily appreciate that theteachings found herein may be applied to yet other embodiments withinthe scope of the claims hereto attached. The complete disclosure of allpatents, patent documents, and publications are incorporated herein byreference as if individually incorporated.

What is claimed is:
 1. A coating composition consisting of: water; alatex polymer stabilized with an alkali-soluble polymer; wherein thealkali-soluble polymer is derived from greater than 10% by weight of oneor more polymerizable acid monomers; wherein the latex polymer comprisesone or more acetoacetyl-functional groups of the formula:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup; trimethylolpropane ethoxylate tri(meth)acrylate; and a hydrogenabstraction-type photoinitiator; wherein the hydrogen abstraction-typephotoinitiator is selected to cure the acetoacetyl-functional latexpolymer via a free radical UV cure mechanism through hydrogenabstraction of the —C(O)—CH₂—C(O)— hydrogens; wherein the coatingcomposition does not include a multifunctional amine crosslinker.
 2. Thecoating composition of claim 1 comprising no more than 10 wt-% volatileorganic compounds, based on the total weight of the composition.
 3. Thecoating composition of claim 1 wherein the acetoacetyl-functionalpolymer comprises an acetoacetyl-functional polyurethane, epoxy,polyamide, chlorinated polyolefin, acrylic, oil-modified polymer,polyester, or mixtures or copolymers thereof.
 4. The coating compositionof claim 1 wherein the acetoacetyl-functional polymer comprises anacetoacetyl-functional latex polymer prepared from ethylenicallyunsaturated monomers.
 5. The coating composition of claim 4 wherein thelatex polymer comprises particles having an average particle size ofless than 75 nm.
 6. The coating composition of claim 1 wherein theacetoacetyl-functional group is incorporated into the latex polymerusing 2-(acetoacetoxy) ethyl methacrylate, t-butyl acetoacetate,diketene, or combinations thereof.
 7. The coating composition of claim 1wherein the hydrogen abstraction-type photoinitiator is benzophenone or4-methylbenzophenone.
 8. The coating composition of claim 7 which is atleast partially curable by ultraviolet or visible light.
 9. A method ofcoating a substrate, the method comprising applying the coatingcomposition of claim 1 to a substrate and allowing the coatingcomposition to harden.
 10. A coating on a substrate preparable by themethod of claim
 9. 11. The coating composition of claim 1 whereintrimethylolpropane ethoxylate tri(meth)acrylate is present in an amountof at least 5 wt-%, based on the combined weight of trimethylolpropaneethoxylate tri(meth)acrylate and the acetoacetyl-functional polymer. 12.The coating composition of claim 11 wherein the acetoacetyl-functionalpolymer is present in an amount of at least 30 wt-% and no more than 95wt-%, and trimethylolpropane ethoxylate tri(meth)acrylate is present inan amount of at least 5 wt-% and no more than 70 wt-%, based on thecombined weight of trimethylolpropane ethoxylate tri(meth)acrylate andthe acetoacetyl-functional polymer.
 13. The coating composition of claim11 wherein trimethylolpropane ethoxylate tri(meth)acrylate is present inan amount of at least 7.5 wt-%, based on the combined weight oftrimethylolpropane ethoxylate tri(meth)acrylate and theacetoacetyl-functional polymer.
 14. The coating composition of claim 11wherein trimethylolpropane ethoxylate tri(meth)acrylate is present in anamount of at least 10 wt-%, based on the combined weight oftrimethylolpropane ethoxylate tri(meth)acrylate and theacetoacetyl-functional polymer.
 15. The coating composition of claim 1wherein the latex polymer is distinct from the alkali-soluble polymer.16. A method of coating a substrate surface, the method comprising:providing a coating composition consisting of: water; a latex polymerstabilized with an alkali-soluble polymer; wherein the alkali-solublepolymer is derived from greater than 10% by weight of one or morepolymerizable acid monomers; wherein the latex polymer comprises one ormore acetoacetyl-functional groups of the formula:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup; an ethylenically unsaturated compound distinct from the polymercomprising acetoacetyl functionality; wherein the ethylenicallyunsaturated compound is a monomer, oligomer, or mixture thereofcomprising a multifunctional (meth)acrylate-functional monomer selectedfrom the group consisting of isobornyl (meth)acrylate, isodecyl(meth)acrylate, phenoxyethyl (meth)acrylate, trimethylolpropanetri(meth)acrylate, trimethylolpropane ethoxylate tri(meth)acrylate,tripropylene glycol di(meth)acrylate, hexanediol di(meth)acrylate,tetrahydrofurfuryl (meth)acrylate, beta-carboxyethyl (meth)acrylate,bisphenol A ethoxylate di(meth)acrylate, ethoxylated neopentyl glycoldi(meth)acrylate, propoxylated neopentyl glycol di(meth)acrylate,di-(trimethylolpropane tetra (meth)acrylate), pentaerythritoltri(meth)acrylate, pentaerythritol tetra(meth)acrylate, and mixturesthereof; and optionally an initiator; applying the coating compositionto a substrate surface; and at least partially curing the coatingcomposition.
 17. The method of claim 16 wherein the coating compositioncomprises no more than 10 wt-% volatile organic compounds, based on thetotal weight of the composition.
 18. The method of claim 16 wherein theacetoacetyl-functional polymer comprises an acetoacetyl-functionalpolyurethane, epoxy, polyamide, chlorinated polyolefin, acrylic,oil-modified polymer, polyester, or mixtures or copolymers thereof. 19.The method of claim 16 wherein the latex polymer comprises particlescomprising the acetoacetyl-functional polymer, the alkali-solublepolymer, and the ethylenically unsaturated monomer, oligomer, or mixturethereof.
 20. The method of claim 19 wherein the latex polymer comprisesparticles having an average particle size of less than 75 nm.
 21. Themethod of claim 16 wherein the acetoacetyl-functional polymer is presentin an amount of at least 30 wt-% and no more than 95 wt-%, based on thecombined weight of ethylenically unsaturated monomer, oligomer, ormixture thereof and the acetoacetyl-functional polymer, and wherein theethylenically unsaturated monomer, oligomer, or mixture thereof ispresent in an amount of at least 5 wt-% and no more than 70 wt-%, basedon the combined weight of the ethylenically unsaturated monomer,oligomer, or mixture thereof and the acetoacetyl-functional polymer. 22.The method of claim 16 wherein the acetoacetyl functionality isincorporated into the latex polymer using 2-(acetoacetoxy)ethylmethacrylate, t-butyl acetoacetate, or diketene.
 23. The method ofclaim 16 wherein the initiator is present in the latex polymer andcomprises a photoinitiator, wherein the photoinitiator comprisesbenzophenone, 4-methylbenzophenone, benzoyl benzoate,phenylacetophenones, 2,2-dimethoxy-2-phenylacetophenone,alpha,alpha-diethoxyacetophenone, hydroxycyclo-hexylphenylketone,2-hydroxy-2-methyl-1-phenylpropan-1-one,bis-(2,6-dimethoxybenzoyl)-2,4,4-trimethylpentyl phosphine oxide,2,4,6-trimethylbenzoyl-diphenylphosphine oxide, or combinations thereof.24. The method of claim 16 wherein the initiator is present in the latexpolymer and comprises a photoinitiator, wherein the photoinitiator is ahydrogen abstraction-type photoinitiator.
 25. The method of claim 24wherein the hydrogen abstraction-type photoinitiator is benzophenone or4-methylbenzophenone.
 26. The method of claim 16, the method comprisingexposing the coating composition to ultraviolet or visible light.
 27. Acoating on a substrate preparable by the method of claim
 26. 28. Themethod of claim 16 wherein the initiator is present in the latex polymerand comprises a photoinitiator; and wherein at least partially curingthe coating composition comprises applying ultraviolet or visible lightto the coating composition.
 29. The method of claim 16 wherein theethylenically unsaturated monomer, oligomer, or mixture thereof ispresent in an amount of at least 5 wt-%, based on the combined weight ofthe ethylenically unsaturated monomer, oligomer, or mixture thereof andthe acetoacetyl-functional polymer.
 30. The method of claim 29 whereinthe ethylenically unsaturated monomer, oligomer, or mixture thereof ispresent in an amount of at least 7.5 wt-%, based on the combined weightof the ethylenically unsaturated monomer, oligomer, or mixture thereofand the acetoacetyl-functional polymer.
 31. The method of claim 30wherein the ethylenically unsaturated monomer, oligomer, or mixturethereof is present in an amount of at least 10 wt-%, based on thecombined weight of the ethylenically unsaturated monomer, oligomer, ormixture thereof and the acetoacetyl-functional polymer.
 32. The methodof claim 16 wherein the latex polymer is distinct from thealkali-soluble polymer.
 33. A coating composition consisting essentiallyof: water; a latex polymer stabilized with an alkali-soluble polymer;wherein the alkali-soluble polymer is derived from greater than 10% byweight of one or more polymerizable acid monomers; wherein the latexpolymer comprises one or more acetoacetyl-functional groups of theformula:

wherein R¹ is a C1 to C22 alkylene group and R² is a C1 to C22 alkylgroup; and trimethylolpropane ethoxylate tri(meth)acrylate; and ahydrogen abstraction-type photoinitiator; wherein the hydrogenabstraction-type photoinitiator is selected to cure theacetoacetyl-functional latex polymer via a free radical UV curemechanism through hydrogen abstraction of the —C(O)—CH₂—C(O)— hydrogens;wherein the coating composition does not include a multifunctional aminecrosslinker.